US5607908A - Composition for cleaning contact lenses - Google Patents
Composition for cleaning contact lenses Download PDFInfo
- Publication number
- US5607908A US5607908A US08/407,519 US40751995A US5607908A US 5607908 A US5607908 A US 5607908A US 40751995 A US40751995 A US 40751995A US 5607908 A US5607908 A US 5607908A
- Authority
- US
- United States
- Prior art keywords
- radical
- sub
- independently
- integer
- contact lens
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 238000004140 cleaning Methods 0.000 title claims abstract description 38
- 239000004094 surface-active agent Substances 0.000 claims abstract description 54
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 41
- 230000000694 effects Effects 0.000 claims abstract description 12
- 239000007864 aqueous solution Substances 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims description 18
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 239000004599 antimicrobial Substances 0.000 claims description 7
- 238000009736 wetting Methods 0.000 claims description 7
- 239000010452 phosphate Substances 0.000 claims description 6
- 239000006172 buffering agent Substances 0.000 claims description 5
- 229940117927 ethylene oxide Drugs 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 239000000080 wetting agent Substances 0.000 claims description 5
- 101150108015 STR6 gene Proteins 0.000 claims 1
- 230000000249 desinfective effect Effects 0.000 claims 1
- 239000012929 tonicity agent Substances 0.000 claims 1
- -1 polyoxyethylene Polymers 0.000 description 17
- 239000000463 material Substances 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 10
- 239000012459 cleaning agent Substances 0.000 description 9
- 230000007794 irritation Effects 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 125000002091 cationic group Chemical group 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 7
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
- 229920002050 silicone resin Polymers 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 229920002413 Polyhexanide Polymers 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
- 150000002632 lipids Chemical class 0.000 description 5
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
- 229910052700 potassium Inorganic materials 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 5
- 229910003202 NH4 Inorganic materials 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 229910052744 lithium Inorganic materials 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 229920001983 poloxamer Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N 1-dodecanol group Chemical class C(CCCCCCCCCCC)O LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 3
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000001923 methylcellulose Substances 0.000 description 3
- 235000010981 methylcellulose Nutrition 0.000 description 3
- 231100000344 non-irritating Toxicity 0.000 description 3
- 229920000136 polysorbate Polymers 0.000 description 3
- 239000001103 potassium chloride Substances 0.000 description 3
- 235000011164 potassium chloride Nutrition 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 101000618467 Hypocrea jecorina (strain ATCC 56765 / BCRC 32924 / NRRL 11460 / Rut C-30) Endo-1,4-beta-xylanase 2 Proteins 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 229960003260 chlorhexidine Drugs 0.000 description 2
- 239000000882 contact lens solution Substances 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000017 hydrogel Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 150000002829 nitrogen Chemical class 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical class CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- HLHOHTNONYACFD-UHFFFAOYSA-N 1-[4-[4-morpholin-4-yl-1-[1-(pyridine-3-carbonyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C=1C=C(C=2N=C3N(C4CCN(CC4)C(=O)C=4C=NC=CC=4)N=CC3=C(N3CCOCC3)N=2)C=CC=1NC(=O)NC1=CC=NC=C1 HLHOHTNONYACFD-UHFFFAOYSA-N 0.000 description 1
- RXGSAYBOEDPICZ-UHFFFAOYSA-N 2-[6-[[amino-(diaminomethylideneamino)methylidene]amino]hexyl]-1-(diaminomethylidene)guanidine Chemical compound NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)N RXGSAYBOEDPICZ-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- AEDQNOLIADXSBB-UHFFFAOYSA-N 3-(dodecylazaniumyl)propanoate Chemical compound CCCCCCCCCCCCNCCC(O)=O AEDQNOLIADXSBB-UHFFFAOYSA-N 0.000 description 1
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
- RFRMMZAKBNXNHE-UHFFFAOYSA-N 6-[4,6-dihydroxy-5-(2-hydroxyethoxy)-2-(hydroxymethyl)oxan-3-yl]oxy-2-(hydroxymethyl)-5-(2-hydroxypropoxy)oxane-3,4-diol Chemical compound CC(O)COC1C(O)C(O)C(CO)OC1OC1C(O)C(OCCO)C(O)OC1CO RFRMMZAKBNXNHE-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- 206010015946 Eye irritation Diseases 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- HSHXDCVZWHOWCS-UHFFFAOYSA-N N'-hexadecylthiophene-2-carbohydrazide Chemical compound CCCCCCCCCCCCCCCCNNC(=O)c1cccs1 HSHXDCVZWHOWCS-UHFFFAOYSA-N 0.000 description 1
- 229920002059 Pluronic® P 104 Polymers 0.000 description 1
- 229920001090 Polyaminopropyl biguanide Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229960003333 chlorhexidine gluconate Drugs 0.000 description 1
- YZIYKJHYYHPJIB-UUPCJSQJSA-N chlorhexidine gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.C1=CC(Cl)=CC=C1NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC1=CC=C(Cl)C=C1 YZIYKJHYYHPJIB-UUPCJSQJSA-N 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 229940079886 disodium lauryl sulfosuccinate Drugs 0.000 description 1
- OKBPCTLSPGDQBO-UHFFFAOYSA-L disodium;dichloride Chemical compound [Na+].[Na+].[Cl-].[Cl-] OKBPCTLSPGDQBO-UHFFFAOYSA-L 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940009662 edetate Drugs 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 231100000013 eye irritation Toxicity 0.000 description 1
- ZHPNWZCWUUJAJC-UHFFFAOYSA-N fluorosilicon Chemical compound [Si]F ZHPNWZCWUUJAJC-UHFFFAOYSA-N 0.000 description 1
- ZXWWAOVKKOVZCZ-UHFFFAOYSA-K fluorosilicon(3+) prop-2-enoate Chemical compound C(C=C)(=O)[O-].F[Si+3].C(C=C)(=O)[O-].C(C=C)(=O)[O-] ZXWWAOVKKOVZCZ-UHFFFAOYSA-K 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 150000002303 glucose derivatives Chemical class 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 239000008266 hair spray Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940071190 laureth sulfosuccinate Drugs 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 229940031722 methyl gluceth-20 Drugs 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- BOUCRWJEKAGKKG-UHFFFAOYSA-N n-[3-(diethylaminomethyl)-4-hydroxyphenyl]acetamide Chemical compound CCN(CC)CC1=CC(NC(C)=O)=CC=C1O BOUCRWJEKAGKKG-UHFFFAOYSA-N 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical group 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229960000502 poloxamer Drugs 0.000 description 1
- 229920001992 poloxamer 407 Polymers 0.000 description 1
- 229940093424 polyaminopropyl biguanide Drugs 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229950008882 polysorbate Drugs 0.000 description 1
- 229940068977 polysorbate 20 Drugs 0.000 description 1
- 229940068965 polysorbates Drugs 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- SOGFHWHHBILCSX-UHFFFAOYSA-J prop-2-enoate silicon(4+) Chemical compound [Si+4].[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C SOGFHWHHBILCSX-UHFFFAOYSA-J 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229940102541 sodium trideceth sulfate Drugs 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- KLYDBHUQNXKACI-UHFFFAOYSA-M sodium;2-[2-(2-tridecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O KLYDBHUQNXKACI-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
- C11D3/3738—Alkoxylated silicones
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0078—Compositions for cleaning contact lenses, spectacles or lenses
Definitions
- This invention relates to a composition for cleaning contact lenses which comprises a silicone surface active agent having cleaning activity for contact lens deposits.
- Deposits from the tear film include protein, lipid and mucin, and deposits from external sources include cosmetic deposits, such as from mascara or hair spray, or materials deposited when the lens is handled.
- Surfactant contact lens cleaners which employ a surface active agent having cleaning action, are used to remove lipid deposits, loosely bound protein deposits, and other deposits.
- Surfactant cleaners are used for hard and soft contact lenses.
- Hard lenses include polymethylmethacrylate lenses and rigid gas permeable (RGP) lenses formed of a silicon acrylate type or a fluorosilicon acrylate type polymer.
- Soft lenses include hydrophilic hydrogel lenses.
- Surfactant cleaners are generally used in conjunction with finger rubbing or other mechanical cleaning, followed by rinsing to remove the deposits.
- a wide variety of surface active agents are known for use as a primary cleaning agent in contact lens cleaning compositions, including various anionic, cationic, nonionic or amphoteric surface active agents, and certain combinations thereof.
- compositions for cleaning soft and silicone contact lenses which contain a polyoxyalkylene modified silicone resin and at least one fatty acid amide or nitrogen analog thereof. Additionally, compositions for cleaning machined lens blanks are described which do not employ any silicone resin and include a combination of the amides or nitrogen analogs as the primary cleaning agent.
- the described silicone resins are preferably block copolymers having the formula:
- T is alkyl of from 1 to 3 carbon atoms, usually methyl
- T' is alkyl of from 1 to 6 carbon atoms, usually 3 to 4 carbon atoms
- n is an integer of from 2 to 30, and x and y are numbers within various ranges.
- the silicone resin in the Chen patent was reported as not particularly effective as a primary cleaning agent for contact lens deposits. Additionally, the compositions described in the Sibley et al. patents which include the described silicone resin require the inclusion of the amide surfactant as a primary cleaning agent.
- this invention provides an aqueous composition for cleaning contact lenses which comprises a silicone surface active agent having cleaning activity for contact lens deposits.
- the silicone surface active agent has at least one side chain including a radical ionizable in aqueous solution.
- the invention relates to compositions for cleaning contact lenses which comprise the silicone surface active agent and an antimicrobial agent, and compositions for cleaning and wetting contact lenses which comprise the silicone surface active agent.
- the invention relates to methods employing the compositions.
- the cleaning composition of the invention is an aqueous composition which comprises a silicone surface active agent having cleaning action for contact lens deposits.
- the silicone surface active agent is a silicone polymer having at least one side chain including a radical ionizable in aqueous solution.
- silicone surface active agents are represented by Formula (I): ##STR1## wherein: each R is independently selected from the group consisting of C 1 -C 11 alkyl and phenyl, preferably methyl;
- each R 2 is independently a radical having the formula
- each R 3 is independently a radical having the formula
- each R 4 is independently an alkylene radical having 1 to 6 carbon atoms
- each EO is the ethyleneoxide radical --(C 2 H 4 O)--, preferably --(CH 2 CH 2 O)--;
- each PO is the propyleneoxide radical --(C 3 H 6 O)--, preferably --(CH 2 CH(CH 3 )O)--;
- each Z is independently a radical ionizable in aqueous solution
- a is 0 or an integer of at least 1, preferably 0 to 200;
- b is 0 or an integer of at least 1, preferably 0 to 200;
- c is an integer of at least 1, preferably 1 to 200;
- each of x, y and z is independently 0 or an integer of at least 1, preferably 0 to 20.
- compositions provide desired cleaning activity for a wide variety of contact lens deposits.
- the present compositions may include the described silicone surface active agent as the primary cleaning agent, i.e., the compositions of the invention do not require another surface active cleaning agent such as the amide surface active agent required in the compositions of U.S. Pat. Nos. 4,048,122 and 4,126,587.
- the silicone surface active agents contribute to the ability of compositions to wet surfaces of contact lenses treated with the compositions. More specifically, it appears that when lenses are treated with the compositions, the hydrophobic silicone portion of these polymers may loosely associate with the lens surface, whereby the pendant side chain extends from the lens surface to enhance wettability of the lens surface.
- compositions which are sufficiently nonirritating that a contact lens treated with the composition can be inserted directly on the eye.
- the composition can be used for both cleaning and the subsequent rinsing of a contact lens to remove debris, or for cleaning and wetting a contact lens, wherein the contact lens exposed to the composition can be inserted directly in the eye.
- the silicone surface active agent is a surface active agent having cleaning activity composed of a silicone backbone having one or more pendant side chains including the ionizable radical.
- Preferred agents include dimethylpolysiloxanes wherein at least one methyl group attached to silicon is replaced with the side chain containing the ionizable radical, such as the R 3 side chain and the optional R 2 side chain in Formula (I).
- the R 3 side chains include a functional Z radical which is ionizable in aqueous solution, i.e., the Z radical includes an anionic functional group, a cationic functional group, or an amphoteric functional group.
- the Z radical includes an anionic functional group, a cationic functional group, or an amphoteric functional group.
- These functional ionizable groups render the silicone agent anionic, cationic or amphoteric, depending on the specific functional Z group.
- Silicone surface active agents employed in the compositions are known or can be prepared by methods known to persons skilled in the art, and many of the agents are commercially available.
- Silicone surface active agents contemplated for the compositions include the following: the silicone phosphobetaines described in U.S. Pat. No. 5,091,493 (O'Lenick, Jr. et al.); the silicone phosphate amines described in U.S. Pat. No. 5,093,452 (O'Lenick, Jr.); the ether amine silicone polymers described in U.S. Pat. No. 5,070,168 (O'Lenick, Jr.); the sulfonated silicone polymers described in U.S. Pat. No.
- a preferred class of silicone surface active agents includes surface active agents which have a ionizable Z radical containing a sulfonate radical or a sulfosuccinate radical.
- Illustrative Z radicals ##STR2## wherein in the above formulae, each M is independently selected from the group consisting of H, Na, K, Li and NH 4 .
- Dimethylpolysiloxane polymers containing a pendant side chain having a sulfonate or sulfosuccinate radical are available under the tradenames Silube WS-100 and Silube SS-154-100 from Siltech, Inc., Norcross, Ga., U.S.A.
- silicone surface active agents include surface active agents having an ionizable Z radical containing a phosphate radical.
- phosphobetaines which include a Z radical of the formula: ##STR3## wherein R 6 is a quaternary ammonium radical, e is 1 or 2, f is 0 or 1, and the sum of e and f is 2; and M is selected from the group consisting of H, Na, K, Li and NH 4 .
- Dimethylpolysiloxanes containing a pendant side chain with a phosphobetaine radical are available under the tradename Silicone Phosphobetaine from Siltech, Inc.
- silicone surface active agents include silicone surface active agents containing a Z radical of the formula: ##STR4## wherein M is selected from the group consisting of H, Na, K, Li and NH 4 , such as the dimethylpolysiloxane substituted with propyleneglycol betaine available under the tradename Abil B 9950 from Goldschmidt Chemical Corp., Hopewell, Va., U.S.A; and silicone agents containing a Z radical of the formula:
- q is 1 or 2
- r is 0 or 1, and the sum of q and r is 2
- M is selected from the group consisting of H, Na, K, Li and NH 4 , such as the dimethylpolysiloxanes available under the tradename Siltech Amphoteric from Siltech, Inc.
- silicone surface active agent In addition to the silicone surface active agent, other surface active agents may optionally be employed in the compositions.
- surface active cleaners are known in the art, including anionic, cationic, nonionic and amphoteric surface active agents.
- anionic surface active agents include sulfated and sulfonated surface active agents, and physiologically acceptable salts thereof, which provide good cleaning activity for lipids, proteins, and other contact lens deposits.
- Examples include sodium lauryl sulfate, sodium laureth sulfate (sodium salt of sulfated ethoxylated lauryl alcohol), ammonium laureth sulfate (ammonium salt of sulfated ethoxylated lauryl alcohol), sodium trideceth sulfate (sodium salt of sulfated ethoxylated tridecyl alcohol), sodium dodecylbenzene sulfonate, disodium lauryl or laureth sulfosuccinate (disodium salt of a lauryl or ethoxylated lauryl alcohol half ester of sulfosuccinic acid), disodium oleamido sulfosuccinates, and dio
- Nonionic surface active agents having good cleaning activity include certain polyoxyethylene, polyoxypropylene block copolymer (poloxamer) surface active agents, including various surface active agents available under the tradename Pluronic from BASF Corp., e.g., Pluronic P104 or L64.
- the poloxamers which may be employed as a primary cleaning agent in the compositions of this invention have an HLB value less than 18, generally about 12 to about 18.
- Other representative nonionic surface active agents include: ethoxylated alkyl phenols, such as various surface active agents available under the tradenames Triton (Union Carbide, Tarrytown, N.Y., U.S.A.) and Igepal (Rhone-Poulenc, Cranbury, N.J., U.S.A.); polysorbates such as polysorbate 20, including the polysorbate surface active agents available under the tradename Tween (ICI Americas, Inc., Wilmington, Del., U.S.A.); and alkyl glucosides and polyglucosides such as products available under the tradename Plantaren (Henkel Corp., Hoboken, N.J., U.S.A.).
- compositions may include a cationic surface active agent.
- cationic surface active agents include triquaternary phosphate esters, such as various cationic surface active agents available from Mona Industries, Inc., Patterson, N.J., U.S.A. under the tradename Monaquat.
- compositions may include an amphoteric surface active agent.
- Amphoteric surface active agents include fatty acid amide betaines, such as the cocoamidoalkyl betaines available under the tradename Tego-Betain (Goldschmidt Chemical Corp., Hopewell, Va., U.S.A.).
- Other amphoterics include imidazoline derivatives such as cocoamphopropionates available under the tradename Miranol (Rhone-Poulenc), and N-alkylamino acids such as lauramino propionic acid available under the tradename Mirataine (Rhone-Poulenc).
- the surface active agents having cleaning activity for contact lens deposits may be employed at about 0.001 to about 5 weight percent of the composition, preferably at about 0.005 to about 2 weight percent, with about 0.01 to about 0.1 weight percent being especially preferred.
- compositions intended for cleaning and wetting contact lenses may include as necessary a supplemental wetting agent.
- Representative wetting agents include: cellulosic materials such as cationic cellulosic polymers, hydroxypropyl methylcellulose, hydroxyethyl cellulose and methylcellulose; polyvinyl alcohol; polyvinyl pyrrolidone; and silicone polymers containing a pendant alkyleneoxy side chain (particularly, polymers wherein the side chain does not include an ionizable radical). These latter silicone polymers are preferred in that they are especially compatible with the silicone polymers employed as the primary cleaning agent. Additionally, these latter silicone polymers are useful for alleviating eye irritation potential of the compositions.
- a preferred material is Dow Corning® 193 (Dow Corning, Midland, Mich., U.S.A.).
- the compositions may include a polyethyleneoxy (PEO) containing material (in addition to any silicone polymer which contains PEO in the pendant side chain), especially a PEO-containing material having a hydrophile-lipophile balance (HLB) of at least about 18.
- PEO polyethyleneoxy
- HLB hydrophile-lipophile balance
- PEO-containing materials include homopolymers of polyethylene glycol or polyethyleneoxide having the high HLB value, and certain poloxamers such as materials commercially available from BASF under the tradenames Pluronic F108 and Pluronic F127.
- Other preferred PEO-containing materials include ethoxylated glucose derivatives, such as the ethoxylated products available under the tradename Glucam (Amerchol Corp., Edison, N.J., U.S.A.), and high HLB ethoxylated nonionic ethers of sorbitol or glycerol, such as products available under the tradename Ethosperse, including sorbeth-20 supplied as Ethosperse SL-20 and glycereth-26 supplied as Ethosperse G-26 (Lonza Inc., Fair Lawn, N.J., U.S.A.).
- the PEO-containing materials and/or the above-described wetting agents may be used in a wide range of concentrations, generally about 0.1 to about 10 weight percent.
- the compositions include as necessary buffering agents for buffering or adjusting pH of the composition, and/or tonicity adjusting agents for adjusting the tonicity of the composition.
- Representative buffering agents include: alkali metal salts such as potassium or sodium carbonates, acetates, borates, phosphates, citrates and hydroxides; and weak acids such as acetic, boric and phosphoric acids.
- Representative tonicity adjusting agents include: sodium and potassium chloride, and those materials listed as buffering agents.
- the tonicity agents may be employed in an amount effective to adjust the osmotic value of the final composition to a desired value.
- the buffering agents and/or tonicity adjusting agents may be included up to about 10 weight percent.
- an antimicrobial agent is included in the composition in an antimicrobially effective amount, i.e., an amount which is effective to at least inhibit growth of microorganisms in the composition.
- the composition can be used to disinfect a contact lens treated therewith.
- antimicrobial agents are known in the art as useful in contact lens solutions, including: chlorhexidine (1,1'-hexamethylene-bis[5-(p-chlorophenyl)biguanide]) or water soluble salts thereof, such as chlorhexidine gluconate; polyhexamethylene biguanide (PHMB, a polymer of hexamethylene biguanide, also referred to as polyaminopropyl biguanide) or water-soluble salts thereof, such as the polyhexamethylene biguanide hydrochloride available under the trade name Cosmocil CQ (ICI Americas Inc.); benzalkonium chloride; and polymeric quaternary ammonium salts.
- the antimicrobial agent may be included at 0.00001 to about 5 weight percent, depending on the specific agent.
- compositions may further include a sequestering agent (or chelating agent) which can be present up to about 2.0 weight percent.
- sequestering agents include ethylenediaminetetraacetic acid (EDTA) and its salts, with the disodium salt (disodium edetate) being especially preferred.
- Hard lenses include polymethylmethacrylate lenses and rigid gas permeable (RGP) lenses formed of a silicon or a fluorosilicon polymer.
- Soft contact lenses include hydrophilic hydrogel lenses.
- a contact lens is cleaned by exposing the lens to the cleaning composition, preferably by immersing the lens in the composition, followed by agitation, such as by rubbing the composition on the lens surface.
- the lens is then rinsed to remove the composition along with contaminants.
- contact lenses are exposed to the compositions, either by employing the composition to rinse the lenses or by soaking the lenses in the composition.
- the lens can then be inserted directly in the eye.
- compositions listed in the following tables can be prepared by the following general procedure.
- compositions can be prepared by adding the individual components to water.
- a representative method follows.
- the salts and wetting agents such as sodium chloride, potassium chloride, disodium edetate, cellulosic components, and/or polyvinyl alcohol (PVA), are added to premeasured, heated water with mixing.
- This first composition is allowed to cool, filtered, and sterilized.
- the sodium phosphate, potassium phosphate, PEO-containing material, the silicone polymer, the surface active agents and/or glycerin are added to premeasured water with mixing and then sterilized and filtered.
- the antimicrobial agents are added to the remaining amount of premeasured water, and the three compositions are combined with mixing.
- compositions of Examples 1 to 8 were tested for cleaning efficacy by the following procedure.
- the surfaces of fluorosilicone RGP contact lenses were contaminated with Vaseline® Intensive Care lotion.
- the surfaces of RGP contact lenses were contaminated with lanolin.
- the contaminated lenses were rubbed with the subject composition, rinsed with water, and inspected visually.
- Each of the compositions provided excellent cleaning of the contact lenses.
- compositions of Examples 1 to 4 were tested according to the following procedure on twenty wearers of RGP contact lenses. First, each subject's lenses were soaked in a composition for at least five minutes, and then the soaked lenses were inserted directly (i.e., without rinsing) onto the subject's eye. The amount of irritation occurring within the first 20-30 seconds after insertion was rated by the subjects using the following scale:
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Abstract
A composition for cleaning contact lenses comprises a silicone surface active agent having cleaning activity for contact lens deposits. The silicone surface active agent has at least one side chain including a radical ionizable in aqueous solution.
Description
This is a divisional of application Ser. No. 08/080,424 filed on Jun. 18, 1993, now U.S. Pat. No. 5,422,029.
This invention relates to a composition for cleaning contact lenses which comprises a silicone surface active agent having cleaning activity for contact lens deposits.
The tendency of contact lens materials to form deposits necessitates regular cleaning of the contact lenses. Deposits from the tear film include protein, lipid and mucin, and deposits from external sources include cosmetic deposits, such as from mascara or hair spray, or materials deposited when the lens is handled.
Surfactant contact lens cleaners, which employ a surface active agent having cleaning action, are used to remove lipid deposits, loosely bound protein deposits, and other deposits. Surfactant cleaners are used for hard and soft contact lenses. Hard lenses include polymethylmethacrylate lenses and rigid gas permeable (RGP) lenses formed of a silicon acrylate type or a fluorosilicon acrylate type polymer. Soft lenses include hydrophilic hydrogel lenses. Surfactant cleaners are generally used in conjunction with finger rubbing or other mechanical cleaning, followed by rinsing to remove the deposits.
A wide variety of surface active agents are known for use as a primary cleaning agent in contact lens cleaning compositions, including various anionic, cationic, nonionic or amphoteric surface active agents, and certain combinations thereof.
U.S. Pat. Nos. 4,048,122 and 4,126,587 (Sibley et al.) describe compositions for cleaning soft and silicone contact lenses which contain a polyoxyalkylene modified silicone resin and at least one fatty acid amide or nitrogen analog thereof. Additionally, compositions for cleaning machined lens blanks are described which do not employ any silicone resin and include a combination of the amides or nitrogen analogs as the primary cleaning agent. The described silicone resins are preferably block copolymers having the formula:
TSi(O(SiMe.sub.2 O).sub.x (C.sub.n H.sub.2n O).sub.y T'.sub.3
wherein T is alkyl of from 1 to 3 carbon atoms, usually methyl, T' is alkyl of from 1 to 6 carbon atoms, usually 3 to 4 carbon atoms, n is an integer of from 2 to 30, and x and y are numbers within various ranges.
U.S. Pat. No. 4,613,380 (Chen) reports tests evaluating the effectiveness of various agents for removing lipid deposits from silicone elastomer contact lenses. A silicone glycol copolymer (Dow Corning® 190, a silicone polymer containing polyoxyethylene and/or polyoxypropylene side chains), designated in the patent as "Surfactant 1", was employed as a comparative example in tests for effectiveness at removing lipid deposits from the contact lenses.
It will be appreciated that the silicone resin in the Chen patent was reported as not particularly effective as a primary cleaning agent for contact lens deposits. Additionally, the compositions described in the Sibley et al. patents which include the described silicone resin require the inclusion of the amide surfactant as a primary cleaning agent.
In a first aspect, this invention provides an aqueous composition for cleaning contact lenses which comprises a silicone surface active agent having cleaning activity for contact lens deposits. The silicone surface active agent has at least one side chain including a radical ionizable in aqueous solution.
In other aspects, the invention relates to compositions for cleaning contact lenses which comprise the silicone surface active agent and an antimicrobial agent, and compositions for cleaning and wetting contact lenses which comprise the silicone surface active agent.
Additionally, the invention relates to methods employing the compositions.
The cleaning composition of the invention is an aqueous composition which comprises a silicone surface active agent having cleaning action for contact lens deposits. The silicone surface active agent is a silicone polymer having at least one side chain including a radical ionizable in aqueous solution.
Representative silicone surface active agents are represented by Formula (I): ##STR1## wherein: each R is independently selected from the group consisting of C1 -C11 alkyl and phenyl, preferably methyl;
each R2 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --H;
each R3 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --Z;
each R4 is independently an alkylene radical having 1 to 6 carbon atoms;
each EO is the ethyleneoxide radical --(C2 H4 O)--, preferably --(CH2 CH2 O)--;
each PO is the propyleneoxide radical --(C3 H6 O)--, preferably --(CH2 CH(CH3)O)--;
each Z is independently a radical ionizable in aqueous solution;
a is 0 or an integer of at least 1, preferably 0 to 200;
b is 0 or an integer of at least 1, preferably 0 to 200;
c is an integer of at least 1, preferably 1 to 200; and
each of x, y and z is independently 0 or an integer of at least 1, preferably 0 to 20.
The compositions provide desired cleaning activity for a wide variety of contact lens deposits. In contrast with the compositions containing the silicone resins described in the aforementioned U.S. Pat. Nos. 4,613,380, 4,048,122 and 4,126,587, the present compositions may include the described silicone surface active agent as the primary cleaning agent, i.e., the compositions of the invention do not require another surface active cleaning agent such as the amide surface active agent required in the compositions of U.S. Pat. Nos. 4,048,122 and 4,126,587.
Additionally, the silicone surface active agents contribute to the ability of compositions to wet surfaces of contact lenses treated with the compositions. More specifically, it appears that when lenses are treated with the compositions, the hydrophobic silicone portion of these polymers may loosely associate with the lens surface, whereby the pendant side chain extends from the lens surface to enhance wettability of the lens surface.
These agents are also relatively nonirritating to the eye, and the invention also relates to compositions which are sufficiently nonirritating that a contact lens treated with the composition can be inserted directly on the eye. For example, the composition can be used for both cleaning and the subsequent rinsing of a contact lens to remove debris, or for cleaning and wetting a contact lens, wherein the contact lens exposed to the composition can be inserted directly in the eye.
The silicone surface active agent is a surface active agent having cleaning activity composed of a silicone backbone having one or more pendant side chains including the ionizable radical. Preferred agents include dimethylpolysiloxanes wherein at least one methyl group attached to silicon is replaced with the side chain containing the ionizable radical, such as the R3 side chain and the optional R2 side chain in Formula (I).
As illustrated in Formula (I), the R3 side chains include a functional Z radical which is ionizable in aqueous solution, i.e., the Z radical includes an anionic functional group, a cationic functional group, or an amphoteric functional group. These functional ionizable groups render the silicone agent anionic, cationic or amphoteric, depending on the specific functional Z group.
The silicone surface active agents employed in the compositions are known or can be prepared by methods known to persons skilled in the art, and many of the agents are commercially available. Silicone surface active agents contemplated for the compositions include the following: the silicone phosphobetaines described in U.S. Pat. No. 5,091,493 (O'Lenick, Jr. et al.); the silicone phosphate amines described in U.S. Pat. No. 5,093,452 (O'Lenick, Jr.); the ether amine silicone polymers described in U.S. Pat. No. 5,070,168 (O'Lenick, Jr.); the sulfonated silicone polymers described in U.S. Pat. No. 4,960,845 (O'Lenick, Jr.); the silicone polymers described in U.S. Pat. No. 5,073,619 (O'Lenick, Jr.); the phosphated silicone polymers described in U.S. Pat. No. 5,070,171 ((O'Lenick, Jr.); and the silicone ester quaternary polymers described in U.S. Pat. No. 5,166,297 (O'Lenick, Jr.).
A preferred class of silicone surface active agents includes surface active agents which have a ionizable Z radical containing a sulfonate radical or a sulfosuccinate radical. Illustrative Z radicals ##STR2## wherein in the above formulae, each M is independently selected from the group consisting of H, Na, K, Li and NH4. Dimethylpolysiloxane polymers containing a pendant side chain having a sulfonate or sulfosuccinate radical are available under the tradenames Silube WS-100 and Silube SS-154-100 from Siltech, Inc., Norcross, Ga., U.S.A.
Another preferred class of silicone surface active agents include surface active agents having an ionizable Z radical containing a phosphate radical. Especially preferred are phosphobetaines which include a Z radical of the formula: ##STR3## wherein R6 is a quaternary ammonium radical, e is 1 or 2, f is 0 or 1, and the sum of e and f is 2; and M is selected from the group consisting of H, Na, K, Li and NH4. Dimethylpolysiloxanes containing a pendant side chain with a phosphobetaine radical are available under the tradename Silicone Phosphobetaine from Siltech, Inc.
Other preferred silicone surface active agents include silicone surface active agents containing a Z radical of the formula: ##STR4## wherein M is selected from the group consisting of H, Na, K, Li and NH4, such as the dimethylpolysiloxane substituted with propyleneglycol betaine available under the tradename Abil B 9950 from Goldschmidt Chemical Corp., Hopewell, Va., U.S.A; and silicone agents containing a Z radical of the formula:
--N(H).sub.q (CH.sub.2 CH.sub.2 COO.sup.- M.sup.+).sub.r
wherein q is 1 or 2, r is 0 or 1, and the sum of q and r is 2; and M is selected from the group consisting of H, Na, K, Li and NH4, such as the dimethylpolysiloxanes available under the tradename Siltech Amphoteric from Siltech, Inc.
In addition to the silicone surface active agent, other surface active agents may optionally be employed in the compositions. A wide variety of surface active cleaners are known in the art, including anionic, cationic, nonionic and amphoteric surface active agents.
Representative anionic surface active agents include sulfated and sulfonated surface active agents, and physiologically acceptable salts thereof, which provide good cleaning activity for lipids, proteins, and other contact lens deposits. Examples include sodium lauryl sulfate, sodium laureth sulfate (sodium salt of sulfated ethoxylated lauryl alcohol), ammonium laureth sulfate (ammonium salt of sulfated ethoxylated lauryl alcohol), sodium trideceth sulfate (sodium salt of sulfated ethoxylated tridecyl alcohol), sodium dodecylbenzene sulfonate, disodium lauryl or laureth sulfosuccinate (disodium salt of a lauryl or ethoxylated lauryl alcohol half ester of sulfosuccinic acid), disodium oleamido sulfosuccinates, and dioctyl sodium sulfosuccinate (sodium salt of the diester of a 2-ethylhexyl alcohol and sulfosuccinic acid).
Nonionic surface active agents having good cleaning activity include certain polyoxyethylene, polyoxypropylene block copolymer (poloxamer) surface active agents, including various surface active agents available under the tradename Pluronic from BASF Corp., e.g., Pluronic P104 or L64. (In contrast with the high-HLB PEO-containing materials, the poloxamers which may be employed as a primary cleaning agent in the compositions of this invention have an HLB value less than 18, generally about 12 to about 18.) Other representative nonionic surface active agents include: ethoxylated alkyl phenols, such as various surface active agents available under the tradenames Triton (Union Carbide, Tarrytown, N.Y., U.S.A.) and Igepal (Rhone-Poulenc, Cranbury, N.J., U.S.A.); polysorbates such as polysorbate 20, including the polysorbate surface active agents available under the tradename Tween (ICI Americas, Inc., Wilmington, Del., U.S.A.); and alkyl glucosides and polyglucosides such as products available under the tradename Plantaren (Henkel Corp., Hoboken, N.J., U.S.A.).
The compositions may include a cationic surface active agent. Representative cationic surface active agents include triquaternary phosphate esters, such as various cationic surface active agents available from Mona Industries, Inc., Patterson, N.J., U.S.A. under the tradename Monaquat.
Additionally, the compositions may include an amphoteric surface active agent. Amphoteric surface active agents include fatty acid amide betaines, such as the cocoamidoalkyl betaines available under the tradename Tego-Betain (Goldschmidt Chemical Corp., Hopewell, Va., U.S.A.). Other amphoterics include imidazoline derivatives such as cocoamphopropionates available under the tradename Miranol (Rhone-Poulenc), and N-alkylamino acids such as lauramino propionic acid available under the tradename Mirataine (Rhone-Poulenc).
The surface active agents having cleaning activity for contact lens deposits, including the silicone cleaning agents, may be employed at about 0.001 to about 5 weight percent of the composition, preferably at about 0.005 to about 2 weight percent, with about 0.01 to about 0.1 weight percent being especially preferred.
As mentioned, the silicone polymers contribute to the ability of the composition to wet surfaces of contact lenses treated therewith. If desired, compositions intended for cleaning and wetting contact lenses may include as necessary a supplemental wetting agent. Representative wetting agents include: cellulosic materials such as cationic cellulosic polymers, hydroxypropyl methylcellulose, hydroxyethyl cellulose and methylcellulose; polyvinyl alcohol; polyvinyl pyrrolidone; and silicone polymers containing a pendant alkyleneoxy side chain (particularly, polymers wherein the side chain does not include an ionizable radical). These latter silicone polymers are preferred in that they are especially compatible with the silicone polymers employed as the primary cleaning agent. Additionally, these latter silicone polymers are useful for alleviating eye irritation potential of the compositions. A preferred material is Dow Corning® 193 (Dow Corning, Midland, Mich., U.S.A.).
Additionally, for compositions intended for application to the eye, such as the cleaning and wetting compositions, the compositions may include a polyethyleneoxy (PEO) containing material (in addition to any silicone polymer which contains PEO in the pendant side chain), especially a PEO-containing material having a hydrophile-lipophile balance (HLB) of at least about 18. These high-HLB PEO-containing materials are useful for further reducing the irritation potential of the surface active agent or other components in the compositions, and in some cases the PEO-containing material may contribute to the wetting ability of the composition. Representative PEO-containing materials include homopolymers of polyethylene glycol or polyethyleneoxide having the high HLB value, and certain poloxamers such as materials commercially available from BASF under the tradenames Pluronic F108 and Pluronic F127. Other preferred PEO-containing materials include ethoxylated glucose derivatives, such as the ethoxylated products available under the tradename Glucam (Amerchol Corp., Edison, N.J., U.S.A.), and high HLB ethoxylated nonionic ethers of sorbitol or glycerol, such as products available under the tradename Ethosperse, including sorbeth-20 supplied as Ethosperse SL-20 and glycereth-26 supplied as Ethosperse G-26 (Lonza Inc., Fair Lawn, N.J., U.S.A.).
When present, the PEO-containing materials and/or the above-described wetting agents may be used in a wide range of concentrations, generally about 0.1 to about 10 weight percent.
The compositions include as necessary buffering agents for buffering or adjusting pH of the composition, and/or tonicity adjusting agents for adjusting the tonicity of the composition. Representative buffering agents include: alkali metal salts such as potassium or sodium carbonates, acetates, borates, phosphates, citrates and hydroxides; and weak acids such as acetic, boric and phosphoric acids. Representative tonicity adjusting agents include: sodium and potassium chloride, and those materials listed as buffering agents. The tonicity agents may be employed in an amount effective to adjust the osmotic value of the final composition to a desired value. Generally, the buffering agents and/or tonicity adjusting agents may be included up to about 10 weight percent.
According to preferred embodiments, an antimicrobial agent is included in the composition in an antimicrobially effective amount, i.e., an amount which is effective to at least inhibit growth of microorganisms in the composition. Preferably, the composition can be used to disinfect a contact lens treated therewith. Various antimicrobial agents are known in the art as useful in contact lens solutions, including: chlorhexidine (1,1'-hexamethylene-bis[5-(p-chlorophenyl)biguanide]) or water soluble salts thereof, such as chlorhexidine gluconate; polyhexamethylene biguanide (PHMB, a polymer of hexamethylene biguanide, also referred to as polyaminopropyl biguanide) or water-soluble salts thereof, such as the polyhexamethylene biguanide hydrochloride available under the trade name Cosmocil CQ (ICI Americas Inc.); benzalkonium chloride; and polymeric quaternary ammonium salts. When present, the antimicrobial agent may be included at 0.00001 to about 5 weight percent, depending on the specific agent.
The compositions may further include a sequestering agent (or chelating agent) which can be present up to about 2.0 weight percent. Examples of preferred sequestering agents include ethylenediaminetetraacetic acid (EDTA) and its salts, with the disodium salt (disodium edetate) being especially preferred.
The compositions are useful for cleaning hard and soft contact lenses. Hard lenses include polymethylmethacrylate lenses and rigid gas permeable (RGP) lenses formed of a silicon or a fluorosilicon polymer. Soft contact lenses include hydrophilic hydrogel lenses.
A contact lens is cleaned by exposing the lens to the cleaning composition, preferably by immersing the lens in the composition, followed by agitation, such as by rubbing the composition on the lens surface. The lens is then rinsed to remove the composition along with contaminants.
For wetting contact lens, contact lenses are exposed to the compositions, either by employing the composition to rinse the lenses or by soaking the lenses in the composition. The lens can then be inserted directly in the eye.
The compositions listed in the following tables can be prepared by the following general procedure.
The compositions can be prepared by adding the individual components to water. A representative method follows. The salts and wetting agents, such as sodium chloride, potassium chloride, disodium edetate, cellulosic components, and/or polyvinyl alcohol (PVA), are added to premeasured, heated water with mixing. This first composition is allowed to cool, filtered, and sterilized. The sodium phosphate, potassium phosphate, PEO-containing material, the silicone polymer, the surface active agents and/or glycerin are added to premeasured water with mixing and then sterilized and filtered. The antimicrobial agents are added to the remaining amount of premeasured water, and the three compositions are combined with mixing.
TABLE I ______________________________________ Component EX 1 EX 2 EX 3 EX 4 ______________________________________ sodium 0.70 0.70 0.70 0.70 chloride potassium 0.040 0.040 0.040 0.040 chloride disodium 0.050 0.050 0.050 0.050 edetate hydroxypropyl 0.60 0.60 0.60 0.60 methylcellulose sodium 0.55 0.55 0.55 0.55 phosphate potassium 0.11 0.11 0.11 0.11 phosphate polyethylene 0.10 0.10 0.10 0.10 glycol (Polyox-WSR 301, 1%, Union Carbide) glycerin 0.050 0.050 0.050 0.050 alkoxylate silicone 0.015 0.015 0.015 0.015 polymer (193, Dow Corning) amphoteric 0.030 -- -- -- polysiloxane (Siltech-Ampho, Siltech) sulfosuccinate -- 0.030 -- polysiloxane (Silube SS-154-00, Siltech) silicone betaine -- -- 0.030 -- (Abil B 9950, Goldschmidt) phosphobetaine -- -- -- 0.030 polysiloxane (Siltech Phosphobetaine) PHMB 0.003 0.003 0.003 0.003 (Cosmocil CQ, 20%, ICI Americas) Deionized Water 100 100 100 100 (q.s. to) ______________________________________
TABLE 2 ______________________________________ Component EX 5 EX 6 EX 7 EX 8 ______________________________________ sodium chloride 0.70 0.70 0.70 0.70 potassium chloride 0.040 0.040 0.040 0.040 disodium edetate 0.050 0.050 0.050 0.050 hydroxypropyl 0.60 0.60 0.60 0.55 methylcellulose sodium phosphate 0.55 0.55 0.55 0.55 potassium phosphate 0.11 0.11 0.11 0.11 polyethylene glycol 0.10 0.10 0.10 -- (1%, Polyox-WSR 301) methyl gluceth-20 -- -- -- 0.10 (Glucam E-20, Amerchol) PVA 1.50 -- -- -- glycerin 0.050 0.050 0.050 -- alkoxylated silicone 0.015 0.015 0.015 0.015 polymer (193, Dow Corning) Siltech-Ampho 0.020 -- -- 0.020 Silube SS-154-00 -- 0.020 -- -- Abil B 9950 -- -- 0.020 -- PHMB (20%) 0.003 0.003 0.003 0.025 chlorhexidine -- -- -- 0.0165 gluconate (20%) Deionized Water 100 100 100 100 (q.s. to) pH 7.3 7.3 7.3 7.3 Viscosity (cp 25° C.) 45.9 41.4 45.1 34.6 Osmolality 364 369 366 366 ______________________________________
The compositions of Examples 1 to 8 were tested for cleaning efficacy by the following procedure. The surfaces of fluorosilicone RGP contact lenses were contaminated with Vaseline® Intensive Care lotion. In separate tests, the surfaces of RGP contact lenses were contaminated with lanolin. The contaminated lenses were rubbed with the subject composition, rinsed with water, and inspected visually. Each of the compositions provided excellent cleaning of the contact lenses.
Additionally, the compositions of Examples 1 to 4 (Table 1) were tested according to the following procedure on twenty wearers of RGP contact lenses. First, each subject's lenses were soaked in a composition for at least five minutes, and then the soaked lenses were inserted directly (i.e., without rinsing) onto the subject's eye. The amount of irritation occurring within the first 20-30 seconds after insertion was rated by the subjects using the following scale:
0=no irritation
2=very mild irritation
3
4=mild irritation
5
6=moderate irritation
7
8=severe irritation
Additionally, five drops of each composition were then instilled directly into both eyes of each subject (one drop every 5 minutes). Again, the amount of irritation occurring within the first 20-30 minutes after instillation of each drop was rated using the above scale.
The entire procedure was repeated on separate days until each subject had tested each composition. The average rating at insertion and following instillation of each drop is listed in Table 4. The data demonstrate that the compositions were substantially nonirritating to the eye.
TABLE 4 ______________________________________ Average Irritation Rating Drop Number Overall Comp Insertion 1 2 3 4 5 Average ______________________________________ EX 1 0.9 1.5 1.2 1.4 1.3 1.5 1.26 EX 2 0.8 0.6 0.8 1.2 1.3 1.4 1.02 EX 3 0.9 0.8 0.9 0.9 0.8 0.8 0.82 EX 4 0.8 0.8 0.7 0.9 1.0 1.0 0.83 ______________________________________
Although certain preferred embodiments have been described, it is understood that the invention is not limited thereto and modifications and variations would be evident to a person of ordinary skill in the art.
Claims (11)
1. A method of cleaning a contact lens comprising exposing a contact lens to an aqueous composition comprising a silicone surface active agent having cleaning activity for contact lens deposits and represented by the formula: ##STR5## wherein: each R is independently selected from the group consisting of C1 -C11 alkyl and phenyl;
each R2 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --H;
each R3 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --Z;
each R4 is independently an alkylene radical having 1 to 6 carbon atoms;
each EO is an ethyleneoxide radical;
each PO is a propyleneoxide radical;
each Z is independently a radical ionizable in aqueous solution;
a is 0 or an integer of at least 1;
b is 0 or an integer of at least 1;
c is an integer of at least 1; and
each of x, y and z is independently 0 or an integer of at least 1.
2. The method of claim 1 wherein said aqueous composition includes at least one of: a wetting agent, an antimicrobial agent, a buffering agent, and a tonicity agent.
3. The method of claim 1 wherein at least one side chain of the silicone polymer contains an ionizable radical selected from at least one of the following: a sulfonate radical, a sulfosuccinate radical, a phosphate radical, and a phosphobetaine radical.
4. The method of claim 1 wherein Z represents a sulfonate radical.
5. The method of claim 1 wherein Z represents a sulfosuccinate radical.
6. The method of claim 1 wherein Z represents a phosphate radical.
7. The method of claim 1 wherein Z represents a phosphobetaine radical.
8. A method of cleaning and disinfecting a contact lens comprising exposing a contact lens to an aqueous composition comprising an antimicrobial agent and silicone surface active agent having cleaning activity for contact lens deposits and represented by the formula: ##STR6## wherein: each R is independently selected from the group consisting of C1 -C11 alkyl and phenyl;
each R2 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --H;
each R3 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --Z;
each R4 is independently an alkylene radical having 1 to 6 carbon atoms;
each EO is an ethyleneoxide radical;
each PO is a propyleneoxide radical;
each Z is independently a radical ionizable in aqueous solution;
a is 0 or an integer of at least 1;
b is 0 or an integer of at least 1;
c is an integer of at least 1; and
each of x, y and z is independently 0 or an integer of at least 1.
9. A method of cleaning and wetting a contact lens comprising rubbing a contact lens with an aqueous composition comprising a silicone surface active agent having cleaning activity for contact lens deposits and represented by the formula: ##STR7## wherein: each R is independently selected from the group consisting of C1 -C11 alkyl and phenyl;
each R2 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --H;
each R3 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --Z;
each R4 is independently an alkylene radical having 1 to 6 carbon atoms;
each EO is an ethyleneoxide radical;
each PO is a propyleneoxide radical;
each Z is independently a radical ionizable in aqueous solution;
a is 0 or an integer of at least 1;
b is 0 or an integer of at least 1;
c is an integer of at least 1; and
each of x, y and z is independently 0 or an integer of at least 1; and
subsequently exposing the contact lens to the aqueous composition to wet a surface of the lens.
10. The method of claim 9, wherein the contact lens is immediately inserted into the eye after the step of rubbing the lens with the aqueous composition.
11. A method of cleaning a contact lens comprising exposing a contact lens to an aqueous composition comprising a silicone surface active agent having cleaning activity for contact lens deposits and represented by the formula: ##STR8## wherein: each R is independently selected from the group consisting of C1 -C11 alkyl and phenyl;
each R2 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --H;
each R3 is independently a radical having the formula
--R.sup.4 --O--(EO).sub.x --(PO).sub.y --(EO).sub.z --Z;
each R4 is independently an alkylene radical having 1 to 6 carbon atoms;
each EO is an ethyleneoxide radical;
each PO is a propyleneoxide radical;
each Z is independently a radical ionizable in aqueous solution and is selected from: a sulfonate radical, a sulfosuccinate radical, a phosphate radical, and a phosphobetaine radical;
a is 0 or an integer of at least 1;
b is 0 or an integer of at least 1;
c is an integer of at least 1; and
each of x, y and z is independently 0 or an integer of at least 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/407,519 US5607908A (en) | 1993-06-18 | 1995-03-16 | Composition for cleaning contact lenses |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/080,424 US5422029A (en) | 1993-06-18 | 1993-06-18 | Composition for cleaning contact lenses |
US08/407,519 US5607908A (en) | 1993-06-18 | 1995-03-16 | Composition for cleaning contact lenses |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US08/080,424 Division US5422029A (en) | 1993-06-18 | 1993-06-18 | Composition for cleaning contact lenses |
Publications (1)
Publication Number | Publication Date |
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US5607908A true US5607908A (en) | 1997-03-04 |
Family
ID=22157284
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/080,424 Expired - Fee Related US5422029A (en) | 1993-06-18 | 1993-06-18 | Composition for cleaning contact lenses |
US08/407,519 Expired - Fee Related US5607908A (en) | 1993-06-18 | 1995-03-16 | Composition for cleaning contact lenses |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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US08/080,424 Expired - Fee Related US5422029A (en) | 1993-06-18 | 1993-06-18 | Composition for cleaning contact lenses |
Country Status (3)
Country | Link |
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US (2) | US5422029A (en) |
AU (1) | AU7247094A (en) |
WO (1) | WO1995000619A1 (en) |
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US5977035A (en) * | 1996-08-30 | 1999-11-02 | Tomey Technology Corporation | Liquid agent for contact lens containing carboxylated amine as a preservative or sterilizing component |
US6063745A (en) * | 1997-11-26 | 2000-05-16 | Allergan | Mutli-purpose contact lens care compositions |
US6425959B1 (en) | 1999-06-24 | 2002-07-30 | Ecolab Inc. | Detergent compositions for the removal of complex organic or greasy soils |
US6444214B1 (en) * | 2000-05-04 | 2002-09-03 | Kimberly-Clark Worldwide, Inc. | Ion-sensitive, water-dispersible polymers, a method of making same and items using same |
US6586377B2 (en) | 1997-11-26 | 2003-07-01 | Advanced Medical Optics, Inc. | Contact lens cleaning compositions |
US20030129083A1 (en) * | 1997-11-26 | 2003-07-10 | Advanced Medical Optics, Inc. | Multi purpose contact lens care compositions including propylene glycol or glycerin |
US20040058073A1 (en) * | 2002-09-20 | 2004-03-25 | Bunyard W. Clayton | Water-dispersible, cationic polymers, a method of making same and items using same |
US20040058600A1 (en) * | 2002-09-20 | 2004-03-25 | Bunyard W. Clayton | Water-dispersible, cationic polymers, a method of making same and items using same |
US20040055704A1 (en) * | 2002-09-20 | 2004-03-25 | Bunyard W. Clayton | Ion triggerable, cationic polymers, a method of making same and items using same |
US20040058606A1 (en) * | 2002-09-20 | 2004-03-25 | Branham Kelly D. | Ion triggerable, cationic polymers, a method of making same and items using same |
US20040063888A1 (en) * | 2002-09-20 | 2004-04-01 | Bunyard W. Clayton | Ion triggerable, cationic polymers, a method of making same and items using same |
US20040062791A1 (en) * | 2002-09-20 | 2004-04-01 | Branham Kelly D. | Ion triggerable, cationic polymers, a method of making same and items using same |
US6790816B2 (en) | 1999-09-24 | 2004-09-14 | Bausch & Lomb Incorporated | High osmolyte cleaning and disinfection method and solution for contact lenses |
US20050288196A1 (en) * | 2004-06-08 | 2005-12-29 | Ocularis Pharma, Inc. | Silicone polymer contact lens compositions and methods of use |
US20060070712A1 (en) * | 2004-10-01 | 2006-04-06 | Runge Troy M | Absorbent articles comprising thermoplastic resin pretreated fibers |
US20060086472A1 (en) * | 2004-10-27 | 2006-04-27 | Kimberly-Clark Worldwide, Inc. | Soft durable paper product |
US20070053948A1 (en) * | 2005-09-08 | 2007-03-08 | Bausch & Lomb Incorporated | Lens care solution demonstration kit |
US20070141936A1 (en) * | 2005-12-15 | 2007-06-21 | Bunyard William C | Dispersible wet wipes with improved dispensing |
US20070148099A1 (en) * | 2005-12-27 | 2007-06-28 | Burke Susan E | Use of aroma compounds as defoaming agents for ophthalmic solutions with high concentrations of surfactants |
US20090173044A1 (en) * | 2008-01-09 | 2009-07-09 | Linhardt Jeffrey G | Packaging Solutions |
US7772138B2 (en) | 2002-05-21 | 2010-08-10 | Kimberly-Clark Worldwide, Inc. | Ion sensitive, water-dispersible polymers, a method of making same and items using same |
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BR9407262A (en) * | 1993-06-18 | 1996-10-01 | Polymer Technology Corp | Aqueous composition and method for cleaning and moistening a contact lens and method for cleaning disinfect and moisten a contact lens |
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FR2771416A1 (en) * | 1997-11-25 | 1999-05-28 | Rhodia Chimie Sa | Anti-misting agents for hard-surface cleaners |
US20080188631A1 (en) * | 2006-10-26 | 2008-08-07 | Power Support Co., Ltd. | Film Coating Liquid |
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US8173147B2 (en) * | 2008-08-15 | 2012-05-08 | Xttrium Laboratories, Inc. | Gentle, non-irritating, non-alcoholic skin disinfectant |
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US5977035A (en) * | 1996-08-30 | 1999-11-02 | Tomey Technology Corporation | Liquid agent for contact lens containing carboxylated amine as a preservative or sterilizing component |
US6063745A (en) * | 1997-11-26 | 2000-05-16 | Allergan | Mutli-purpose contact lens care compositions |
US6319883B1 (en) | 1997-11-26 | 2001-11-20 | Allergan | Multi-purpose contact lens care compositions |
US6482781B2 (en) | 1997-11-26 | 2002-11-19 | Advanced Medical Optics, Inc. | Multi-purpose contact lens care compositions |
US6586377B2 (en) | 1997-11-26 | 2003-07-01 | Advanced Medical Optics, Inc. | Contact lens cleaning compositions |
US20030129083A1 (en) * | 1997-11-26 | 2003-07-10 | Advanced Medical Optics, Inc. | Multi purpose contact lens care compositions including propylene glycol or glycerin |
US6425959B1 (en) | 1999-06-24 | 2002-07-30 | Ecolab Inc. | Detergent compositions for the removal of complex organic or greasy soils |
US6506261B1 (en) | 1999-06-24 | 2003-01-14 | Ecolab Inc. | Detergent compositions for the removal of complex organic or greasy soils |
US6790816B2 (en) | 1999-09-24 | 2004-09-14 | Bausch & Lomb Incorporated | High osmolyte cleaning and disinfection method and solution for contact lenses |
US6814974B2 (en) * | 2000-05-04 | 2004-11-09 | Kimberly-Clark Worldwide, Inc. | Ion-sensitive, water-dispersible polymers, a method of making same and items using same |
US6444214B1 (en) * | 2000-05-04 | 2002-09-03 | Kimberly-Clark Worldwide, Inc. | Ion-sensitive, water-dispersible polymers, a method of making same and items using same |
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US20070010155A1 (en) * | 2002-09-20 | 2007-01-11 | Branham Kelly D | Ion triggerable, cationic polymers, a method of making same and items using same |
US20040058600A1 (en) * | 2002-09-20 | 2004-03-25 | Bunyard W. Clayton | Water-dispersible, cationic polymers, a method of making same and items using same |
US20040062791A1 (en) * | 2002-09-20 | 2004-04-01 | Branham Kelly D. | Ion triggerable, cationic polymers, a method of making same and items using same |
US20040058073A1 (en) * | 2002-09-20 | 2004-03-25 | Bunyard W. Clayton | Water-dispersible, cationic polymers, a method of making same and items using same |
US20040058606A1 (en) * | 2002-09-20 | 2004-03-25 | Branham Kelly D. | Ion triggerable, cationic polymers, a method of making same and items using same |
US6960371B2 (en) | 2002-09-20 | 2005-11-01 | Kimberly-Clark Worldwide, Inc. | Water-dispersible, cationic polymers, a method of making same and items using same |
US20040063888A1 (en) * | 2002-09-20 | 2004-04-01 | Bunyard W. Clayton | Ion triggerable, cationic polymers, a method of making same and items using same |
US6994865B2 (en) | 2002-09-20 | 2006-02-07 | Kimberly-Clark Worldwide, Inc. | Ion triggerable, cationic polymers, a method of making same and items using same |
US20040055704A1 (en) * | 2002-09-20 | 2004-03-25 | Bunyard W. Clayton | Ion triggerable, cationic polymers, a method of making same and items using same |
US7456117B2 (en) | 2002-09-20 | 2008-11-25 | Kimberly-Clark Worldwide, Inc. | Ion triggerable, cationic polymers, a method of making same and items using same |
US7101456B2 (en) | 2002-09-20 | 2006-09-05 | Kimberly-Clark Worldwide, Inc. | Ion triggerable, cationic polymers, a method of making same and items using same |
US7141519B2 (en) | 2002-09-20 | 2006-11-28 | Kimberly-Clark Worldwide, Inc. | Ion triggerable, cationic polymers, a method of making same and items using same |
US7157389B2 (en) | 2002-09-20 | 2007-01-02 | Kimberly-Clark Worldwide, Inc. | Ion triggerable, cationic polymers, a method of making same and items using same |
US20050288196A1 (en) * | 2004-06-08 | 2005-12-29 | Ocularis Pharma, Inc. | Silicone polymer contact lens compositions and methods of use |
US20060070712A1 (en) * | 2004-10-01 | 2006-04-06 | Runge Troy M | Absorbent articles comprising thermoplastic resin pretreated fibers |
US20060086472A1 (en) * | 2004-10-27 | 2006-04-27 | Kimberly-Clark Worldwide, Inc. | Soft durable paper product |
US20070053948A1 (en) * | 2005-09-08 | 2007-03-08 | Bausch & Lomb Incorporated | Lens care solution demonstration kit |
US20070141936A1 (en) * | 2005-12-15 | 2007-06-21 | Bunyard William C | Dispersible wet wipes with improved dispensing |
US20070148099A1 (en) * | 2005-12-27 | 2007-06-28 | Burke Susan E | Use of aroma compounds as defoaming agents for ophthalmic solutions with high concentrations of surfactants |
US20090173044A1 (en) * | 2008-01-09 | 2009-07-09 | Linhardt Jeffrey G | Packaging Solutions |
US7837934B2 (en) | 2008-01-09 | 2010-11-23 | Bausch & Lomb Incorporated | Packaging solutions |
Also Published As
Publication number | Publication date |
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WO1995000619A1 (en) | 1995-01-05 |
US5422029A (en) | 1995-06-06 |
AU7247094A (en) | 1995-01-17 |
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